FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
3M Ioban CHG Chlorhexidine Gluconate Incise Drape (contains 2% w/w CHG)
K Number: K222578
·
Decision May 18, 2023
Classifications
1
FEI Numbers
219
Registration Numbers
219
Same Product Code
449
Applicant Total
50
Review Days
266
Basic Information
- Device Name
- 3M Ioban CHG Chlorhexidine Gluconate Incise Drape (contains 2% w/w CHG)
- K Number
- K222578
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 878.4370
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- 3M Company
- Date Received
- August 25, 2022
- Decision Date
- May 18, 2023
- Product Code
- KKX
- Advisory Committee
- General, Plastic Surgery
- Review Advisory Committee
- HO
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| KKX | Drape, Surgical | FDA class 2 | General, Plastic Surgery |
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